Lev Grinstein
Hamburg, HH 20246, Germany
Last Updated: 09/26/2026
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Found 8 publications
Loss-of-function variant in KCNH3 is associated with global developmental delay, autistic behavior, insomnia, and nocturnal seizures.
Journal: Seizure
Published: January 10, 2025
Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disability.
Journal: American journal of human genetics
Published: July 22, 2024
Association between Tubulointerstitial Nephritis and Uveitis Syndrome and Small-Vessel CNS Vasculitis: A Case of Polyautoimmunity.
Journal: Neuropediatrics
Published: January 05, 2024
P2RX7 gene variants associate with altered inflammasome assembly and reduced pyroptosis in chronic nonbacterial osteomyelitis (CNO).
Journal: Journal of autoimmunity
Published: December 01, 2023
Long-Term Antibody Response to SARS-CoV-2 in Children.
Journal: Journal of clinical immunology
Published: March 04, 2022
Analysis of Activity and Expression of the NLRP3, AIM2, and NLRC4 Inflammasome in Whole Blood.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: February 25, 2022
Thirteen-month-old girl with hyporegenerative macrocytic anemia due to Brown-Vialetto-Van Laere syndrome 2.
Journal: American journal of hematology
Published: February 17, 2022
An optimized whole blood assay measuring expression and activity of NLRP3, NLRC4 and AIM2 inflammasomes.
Journal: Clinical immunology (Orlando, Fla.)
Published: March 13, 2017
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Last Updated: 09/26/2026